CN1234840A - Hollow microfiber and process for preparing same - Google Patents
Hollow microfiber and process for preparing same Download PDFInfo
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- CN1234840A CN1234840A CN98801005A CN98801005A CN1234840A CN 1234840 A CN1234840 A CN 1234840A CN 98801005 A CN98801005 A CN 98801005A CN 98801005 A CN98801005 A CN 98801005A CN 1234840 A CN1234840 A CN 1234840A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
- D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
- D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
- D01F9/127—Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours or other carbon-containing compounds in the form of gas or vapour, e.g. carbon monoxide, alcohols
- D01F9/1273—Alkenes, alkynes
- D01F9/1275—Acetylene
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- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/773—Nanoparticle, i.e. structure having three dimensions of 100 nm or less
- Y10S977/775—Nanosized powder or flake, e.g. nanosized catalyst
- Y10S977/776—Ceramic powder or flake
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
- Y10T428/2909—Nonlinear [e.g., crimped, coiled, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2918—Rod, strand, filament or fiber including free carbon or carbide or therewith [not as steel]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2922—Nonlinear [e.g., crimped, coiled, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2922—Nonlinear [e.g., crimped, coiled, etc.]
- Y10T428/2925—Helical or coiled
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
- Y10T428/2975—Tubular or cellular
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Abstract
A hollow carbon microcoil with the coil pitch of substantially zero, and a hollow ceramic microcoil or a hollow ceramic microfiber prepared by subjecting the hollow carbon microcoil to metallization or other treatments. The hollow carbon microcoil with the coil very densely and orderly wound is characterized by being prepared by strictly regulating reaction conditions in the synthesis of carbon in a microcoil form by catalytically activated thermal decomposition of acetylene and allowing a substrate to descend as the fiber grows. A high-temperature reaction/diffusion treatment of the above hollow carbon microcoil as a starting material in a gas containing various metal components, silicon, boron, carbon, nitrogen and/or oxygen atoms at 800 to 1700 DEG C results in the formation of the hollow ceramic microcoil or microfiber wherein carbon has been reacted or substituted with the starting gas component while completely retaining the hollow of the axis of the fiber.
Description
Invention field
The present invention relates to be applicable to the little coil of hollow of materials such as ternary reinforced composite material, electromagnetic wave absorbent material, electrode material, catalyst, catalyst carrier, adsorbent, micro-mechanical component, microswitching element, microsensor, microfilter or the manufacture method of hollow microfiber.
Background technology
Carbon current fiber, metal carbides or nitride fiber and mono-crystlling fibre (as the elongated monocrystal of cat beard) are to adopt metallic catalyst activation CVD manufactured, and its form is the straight-line fiber that the core of all fibres is full of fully.The fiber axis place has the microtubule shape fiber in cavity not report fully.Generally grow up from fiber and monocrystal that gas phase obtains, but according to this mechanism, what grow into tubulose in theory is impossible according to VLS (gas-liquid-solid) mechanism.As the manufacture method of little coil-like fiber, the present inventor has proposed by earlier in the presence of metallic catalyst and micro-sulphur or phosphorus family impurity, and heating and decomposition acetylene is made the method (opening flat 4-222228 number referring to the spy) of the carbon fiber of little coiled type.Proposed in addition this coiled type carbon fiber is at high temperature handled simultaneously with gas phase coated metal/nitrogenize, thereby obtained the manufacture method (applying for) of the nitride metal fibres of various little coiled types.
The carbon fiber of little coiled type can be by having in the presence of metallic catalyst and micro-sulphur or the phosphorus family impurity, and the heating and decomposition hydrocarbon gas is made, and its repeatability is good and yield is high.Its coil form is generally irregular, or being rule, to curl between coil and coil be not closely to be arranged with the gap.Therefore, study the synthesis condition and the post processing thereof of coiled type carbon fiber in great detail, found that if strict control synthesis condition, what then carbon fiber was fairly regular twists in together, be full of fully between coil, obtain the hollow little carbon fiber of coil axes for the cavity, study the method for making various hollow ceramic microfibers as raw material again, its result is accomplished the present invention.Also can use hollow metal carbide microfiber, metal nitride microfiber, carbonitride microfiber as raw material.The new manufacture method that the purpose of this invention is to provide the hollow microfiber of compound and ceramic compound between a kind of various metallized metal.
Disclosure of the Invention
The present invention relates between fiber axis hollow, coil the little coil of compact arranged hollow form carbon and, be the little coil of hollow ceramic or the hollow ceramic microfiber and the manufacture method thereof of feature with gas phase coated metal, silication, boronation, carbonization, nitrogenize and/or oxidation processes to contain metal, silicon, boron, carbon, nitrogen or to contain in the mist of oxygen atom gas under the high temperature.Further, the present invention relates to little coil of metal carbides or the little coil of metal nitride with the little coil metal generation of hollow form carbon hollow, containing metal, silicon, boron, carbon, nitrogen or containing in the mist of oxygen atom gas under the high temperature, is the little coil of hollow ceramic or the hollow ceramic microfiber and the manufacture method thereof of feature with gas phase coated metal, silication, boronation, carbonization, nitrogenize and/or oxidation processes.
In more detail, the invention provides a kind of in little coiled type carbon building-up process, by strictness control synthesis condition, make and fully closely arrange the little coil of hollow form carbon element that forms between coil, and to provide a kind of be raw material with the little coil of this hollow carbon element, containing various metals under the high temperature, silicon, boron, carbon, nitrogen or contain in the mist of oxygen atom gas, adopt the gas phase diffusion reaction treatment, make part or all and these composition generation physics or chemical reactions of carbon atom, thereby form metallic compound, metal silicide, metal boride, metal carbides, metal nitride, the little coil of the hollow ceramic of metal oxide or its compound.
Further, the invention provides a kind ofly under aforesaid high temperature, adopt the gas phase diffusion reaction treatment, part or all merges with the adjacent windings position of little coil, and part or all that makes little coil becomes fibrous hollow ceramic microfiber.
In addition, it is raw material that the present invention also provides between the known coil of a kind of usefulness little coil of not compact arranged hollow carbon or hollow carbon fiber or hollow carbon microfiber, containing metal under the high temperature, silicon, boron, carbon, nitrogen or contain in the mist of oxygen atom gas, carry out above gas phase treatment of a stage or two stages, make part or all carbon atom and these compositions carry out physics or chemical reaction, thereby form metallic compound, metal silicide, metal boride, metal carbides, metal nitride, the little coil of the hollow ceramic of metal oxide or its compound or hollow ceramic microfiber and manufacture method thereof.
Brief description of drawings
The photo of Fig. 1 is the microphotograph on the hollow titanium nitride microfiber surface that obtains among the embodiment 4.
The photo of Fig. 2 is the mirror ultrafinish section microphotograph of the hollow titanium nitride microfiber that obtains among the embodiment 4.
Implement best mode of the present invention
In the unstrpped gas of using among the present invention, metal ingredient can use the metal simple-substance that at high temperature has high vapour pressure, halide, hydride, organo-metallic compound etc., is so-called transition metal, typical metal, semiconductor alloy, their simple substance and compound basically.As the source of carbon, mainly be to use the carbon atom of carbon fibre, but also can use carbon atoms gases such as hydrocarbon gas such as deriving from outside methane, ethane or carbon tetrachloride.The source of nitrogen element mainly is to use nitrogen, ammonia, acid amides etc. to contain the molecule or the compound of a large amount of nitrogen-atoms.The source of boron mainly is to use boron chloride, diborane, borazine etc. to contain the gaseous compound of boron atom.In addition, element silicon derives from silicon-containing gas such as using silane, disilane, silicon tetrachloride, silicon hexachloride.
In addition, make that to have protium in the reaction system be not necessary especially, but preferably have protium.Also can have inert gases such as He, Ar in the reaction system.In the process of reaction, do not need specially to use catalyst, but can use catalyst necessary the time yet.
When little coil of hollow ceramic among manufacturing the present invention or hollow ceramic microfiber, the raw material that uses can be hollow carbon element microfiber that gas phase is synthetic or the little coil of hollow carbon element, with organic precursor rules such as hollow form graphite fibre, metallic carbide fiber, nitride metal fiber, polyacrylonitrile or pitch, fine and close curling that its heat treatment obtains, form the resulting material of hollow form fiber through moulding, processing, heat treatment.
When making little coil of hollow ceramic of the present invention or hollow ceramic microfiber, reaction temperature is 700-1800 ℃, preferred 900-1200 ℃.The flow of the containing metal composition gas that coated metal is used is the 1-50cc/ branch, preferably at the 5-10cc/ branch.The nitrogen used of nitrogenize or the flow of ammonia are the 10-500cc/ branch in addition, preferred 50-200cc/ branch.The flow of the silicon-containing gas that silication is used is 1-50cc/s, preferred 5-20cc/s.The flow of the boron-containing gas that boronation is used is 1-50cc/s, preferred 5-20cc/s.When reacting under the condition that has hydrogen to exist, the flow of hydrogen is the 250-650cc/ branch, preferred 350-450cc/ branch.When using ammonia, can omit the step that imports hydrogen.Also can in unstrpped gas, add inert gases such as helium, argon.
The fibre diameter of little coil of the hollow that obtains according to the present invention or hollow microfiber is 0.5-15 μ m, and the hollow part diameter is 0.01-5 μ m, and pipe range is in the scope of 0.01-300mm, and is unqualified for these.Owing to the variation that reaction temperature, reaction time or unstrpped gas are formed, can obtain the little coil of hollow ceramic or the hollow ceramic microfiber of residual some carbon atom.
The existence of each element of little coil of hollow ceramic of the present invention or hollow ceramic microfiber there is no need clearly, and coil that is obtained by multicomponent alloy or fiber form various alloying components and become solid solution homogeneous phase, a part of composition or alloying component generation deviation or various structures such as all the components or the fully independent dispersion of alloying component fully.Other compound too.
Little coil of hollow of the present invention or hollow microfiber can be applicable to various uses such as existing linearity carbon fiber, carbide, nitride, boride fiber.Particularly utilizing the various characteristics that specific shape brought of its tubulose, is useful for various function materials such as ternary reinforcing fibers such as FRP and FRM, electromagnetic wave absorbent material, electrode material, micro-mechanical component, microswitching element, microsensor element, microfilter, high temperature corrosion-resisting packaging material, adhesive agent, catalyst material, catalyst carriers.
Specify the present invention below in conjunction with embodiment, but be not limited in the embodiment that mentions.Embodiment 1
In internal diameter 60mm, length 1, the hot CVD device of the longitudinal type suprasil pipe manufacturer of 000mm middle part is placed and is coated with the graphite substrate of having spread nickel powder (average grain diameter is 5 μ m), reacts under 750 ℃.As reacting gas, the acetylene that contains the 1.51mol% thiophene impurities feeds from top with the speed that 200cc/ divides with 400cc/ branch, nitrogen with 80cc/ branch, hydrogen, reacts under normal pressure.The unstripped gas introducing port is 1-10mm, preferred 2-3mm with the distance of the fore-end that generates little coil, along with the generation of coil drops to the position of substrate like this.The coil major part that generates is that two coils curl while growing up, fairly regular, curl and to become double coil very close to each other between the crimped thread circle correctly, closely, the external diameter of coil is that 0.1-15 μ m, coil spacing are 0, loop length depends on the reaction time, generally be 0.01-200mm, so just obtained coil axes and become the empty little coil of hollow carbon element.Embodiment 2
Except catalyst uses titanium and tungsten powder (average grain diameter is 5 μ m), under the condition identical, react with embodiment 1.Can access very fine and close, the gapless double coil between the coil that curls, loop length depends on the reaction time, generally is 0.01-200mm.Embodiment 3
In quartzy alms bowl, add the little coil 100mg of hollow carbon element that embodiment 1 obtains, this quartz alms bowl is placed on the swinging hot CVD device middle part made from the horizontal gyrating type opaque quartz reaction tube of internal diameter 23mm, length 500mm, after in argon gas, being heated to 1200 ℃, dividing feeding titanium tetrachloride gases, 100cc/ to divide with 10cc/ feeds hydrogen, reacted 2 hours.The speed of gyration of reaction tube is 1-300 rev/min, preferred 10-60 rev/min.The weight of reacting rear material increases to 500mg.Adopt the gas phase titanizing to handle the little coil of carbon element, make it from the outside to the inner core, be concentric circles successively by TiCization, adhesion fully between the coil, but kept fully along the axial empty form of fiber.Fully by titanizing, become TiC to its inner core part
1.0The time, its weight is increased to about 5 times.Therefore, according to present embodiment, can obtain the hollow TiC microfiber of 100%TiCization to the fiber inner core.Embodiment 4
Adding embodiment 1 in quartzy alms bowl obtains with the little coil 100mg of hollow carbon element, this quartz alms bowl is placed on the swinging hot CVD device middle part made from the horizontal gyrating type opaque quartz reaction tube of internal diameter 23mm, length 500mm, after in argon gas, being heated to 1200 ℃, dividing feeding titanium tetrachloride gases, 100cc/ to divide with 10cc/ feeds nitrogen, reacted 1 hour.Reacted material becomes dark yellow brown by the grey black look of the little coil of raw material carbon element, weight is increased to 310mg, by its X-ray diffraction pattern, can observe the broad peak shown in the noncrystal phase of the little coil of raw material carbon element, represent the spike that titanium nitride (TiN) exists mutually simultaneously in addition.But the peak that expression titanium carbide (TiC) exists is not mutually observed fully.Just according to present embodiment, the gas phase titanizing and the nitrogenize of the little coil of carbon element are carried out simultaneously, show as by TiNization.When the little coil of carbon element was varied to TiN1.0 fully, weight was about 5.2 times.Therefore, in the present embodiment, the TiN that can be calculated by the weight of increase lead and be about 50%.In addition, reacted material surface and mirror ultrafinish section are as depicted in figs. 1 and 2.The material surface has the TiN particle of particulate polycrystallinity to separate out, and major part is embedded in the ditch of coil and makes its complete adhesion.Observe from its section in addition, can observe in coil surface and the inboard membrane portions existence that continuous white, gloss are arranged, this part is considered to have titanium and nitrogen to exist.On the other hand, think that the core that shades has only carbon element to exist.The TiN part of outside cake round and the area of center carbon element part are 50% than approximately.That is to say, from fiber surface, its cross-sectional area 50% by TiNization, the inner core part still is a carbon element.Can replace nitrogen with ammonia or acid amides gas, almost can access identical result.Embodiment 5
Except that the reaction time is 3 hours, under the condition identical, react with embodiment 4.Reacted material becomes golden yellow by brown.Observe from its section and X-ray diffraction, do not see the existence of the carbon element of the little coil of unreacted hollow carbon element fully, the little coil of raw material carbon element is fully by the TiN membranization.On the other hand, the hollow form of raw material is held fully, becomes the microtubule shape.That is to say, though hollow carbon element coil fully by TiNization, the form of its hollow form also can keep fully, thereby obtains hollow TiN microfiber.Embodiment 6
Remove with zirconium chloride and substitute titanium tetrachloride, the reaction time is beyond 3 hours, reacts under the condition identical with embodiment 4.Reacted material becomes gold by grey, and weight is increased to 8.8 times, can not observe the noncrystal phase of expression material carbon fiber or the peak of ZrC phase by the X-ray diffraction pattern, only to observe the spike that expression ZrN exists mutually.Therefore, in the present embodiment, the variation of material carbon cellulose fiber 100% becomes ZrN.Even the complete ZrNization of the little coil of hollow carbon element, its hollow form form also can keep fully, thereby can access hollow ZrN microfiber.Embodiment 7
Except replacing titanium tetrachloride with columbium pentachloride, the reaction time is beyond 5 hours, reacts under the condition identical with embodiment 4.Can not observe the noncrystal phase of expression material carbon fiber or the peak of NbC phase fully by the X-ray diffraction pattern of reacting rear material.Only to observe the spike that expression NbN exists mutually.Embodiment 8
In quartzy alms bowl, add the hollow form TiC microfiber 100mg that embodiment 3 obtains, this quartz alms bowl is placed on the swinging hot CVD device middle part made from the horizontal gyrating type opaque quartz reaction tube of internal diameter 23mm, length 500mm, after in argon gas, being heated to 1200 ℃, divide the feeding ammonia with 100cc/, reacted 2 hours.Speed of gyration in the course of reaction is 1-300 rev/min, preferred 10-60 rev/min.Reacting rear material becomes golden brown, almost can not observe the increase of weight.But according to the X-ray diffraction pattern, can only observe the peak of titanium nitride phase, can not observe the peak of titanium carbide phase fully.In addition, promptly use nitrogen treatment, the hollow form form of hollow TiC microfiber changes hardly.On the mirror ultrafinish section, be merely able to observe the existence of continuous and thick TiN film, its core full confirmation does not have the existence of carbon element.Embodiment 9
In unstrpped gas, divide to add the methane with 5cc/ in addition, under the condition identical, react with embodiment 4.The color of reacting rear material becomes darkcyan, and weight is increased to 310mg.By the X-ray diffraction pattern, assert except that titanium nitride, to also have the peak of titanium carbide.Embodiment 10
In unstrpped gas, divide to add the steam with 5cc/ in addition, under the condition identical, react with embodiment 4.The color of reacting rear material does not change, and weight is increased to 310mg.By the X-ray diffraction pattern, thinking has the peak of other carbonic acid titanium nitrides of titanium nitride to exist.Embodiment 11
As unstrpped gas, divide to feed titanium tetrachloride, 30cc/ divided by 30cc/ and divide and feed boron chloride, 500cc/ and divide and feed hydrogen, 100cc/ and divide and feed beyond the argon gas, under the condition identical, react with embodiment 3.For reacted material, except that the peak of the noncrystal carbon of the little carbon fibre of hollow that can be observed raw material, also can be observed titanium diboride (TiB by the X-ray diffraction pattern
2) the peak.On the mirror ultrafinish section, the hollow form form of the little coil of raw material hollow carbon element is held fully, thereby obtains the residual hollow titanium diboride microfiber that does not react of a part of the little coil of carbon element.Embodiment 12
Except that the reaction time is 12 hours, under the condition identical, react with embodiment 11.Reacted material to observe the peak of titanium diboride, can not be observed the existence of unreacted carbon element only fully according to the X-ray diffraction pattern.On the mirror ultrafinish section, be merely able to observe the film of continuous titanium diboride, keep fully as the hollow form form of the little coil of hollow carbon element of raw material.That is to say that the little coil of raw material hollow carbon element is converted into titanium diboride fully, thereby obtain hollow titanium diboride microfiber.Embodiment 13
In the middle part of the swinging hot CVD device made from horizontal gyrating type opaque quartz reaction tube of internal diameter 23mm, length 500mm, put into the little coil of hollow carbon element that embodiment 1 obtains, after in argon gas, being heated to 1200 ℃, as unstrpped gas, divide feeding ferric trichloride, 300cc/ to divide with 30cc/ and feed hydrogen, 100cc/ divides the feeding argon gas, reacts 3 hours.The speed of gyration of reaction tube is 1-300 rev/min, preferred 10-60 rev/min.Observe from the X-ray diffraction for reacted material, can confirm except that unreacted carbon element, also have iron and cementite (Fe
3C) existence.Can observe the growth of small crystalline particle on the surface of reaction product, bury between coil fully.Can observe unreacted carbon-coating and cementite layer double-layer structure at the grinding section, in addition, the hollow form of the little coil of raw material hollow carbon element also keeps after reaction fully.Embodiment 14
As unstrpped gas, divide and feed the carbonyl nickel except divide to feed carbonyl iron and 15cc/ with 3cc/, under the condition identical, react with embodiment 13.In reacted material, can confirm that unreacted carbon element is arranged, the existence of iron, cementite and Fe-Ni alloy (Ni:70 wt%).The hollow form of the little coil of raw material hollow carbon element also keeps after reaction fully.Embodiment 15
Except that the reaction time is 12 hours, under the condition identical, react with embodiment 14.In reaction product, unreacted carbon element can not be observed, in addition, one deck Fe-Ni alloy can only be observed on the mirror ultrafinish section.Embodiment 16
The tension intensity of the little coil of hollow carbon element that mensuration embodiment 1 obtains obtains higher value 100-350kg/mm
2(average 250kg/mm
2).Embodiment 17
The tension intensity of the little coil of hollow titanium nitride that mensuration embodiment 5 obtains obtains 50-1 00kg/mm
2(average 70kg/mm
2).Embodiment 18
The resistance value of the little coil of hollow carbon element that mensuration embodiment 1 obtains is 3 * 10
-3Ω cm shows metalline.The resistance value of the hollow titanium carbide microfiber that mensuration embodiment 3 obtains is 1 * 10
-4Ω cm shows metalline fully.Other metal carbides, nitride or metallic compound show the character of metal too.
As mentioned above, adopt acetylene catalyst activation, thermal decomposition, in the time of synthetic little coiled type carbon, by strictness control reaction condition, coil extremely closely, rule, correctly be curled into hollow form, thereby obtain the carbon element coil of microtubule shape.Further, under 800-1800 ℃, in the unstrpped gas that contains various metal ingredients, silicon, boron, carbon, nitrogen or oxygen atom etc., make it to react, can be quantitative obtain its surperficial part or to the ceramic fibre of the microtubule shape of inner core complete reaction.At this time, catalyst is not necessarily necessary especially.
Claims (9)
1. the little coil of hollow form carbon, the pitch essence of coil is 0.
2. the little coil of hollow ceramic, part or all of the little coil of hollow carbon element is metal nitride, metal carbides or carbonitride.
3. the little coil of hollow ceramic as claimed in claim 2 obtains through gas phase coated metal, silication, boronation or oxidation processes.
4. as claim 2 or 3 s' the little coil of hollow ceramic, part or all of its adjacent windings position is fused into the hollow ceramic microfiber.
5. the manufacture method of the little coil of hollow carbon element, it is characterized in that: in method by the synthetic little coil carbon element of catalyst activation CVD method gas phase, in order to make the little coil of carbon element very fine and close, curling regularly, closely arrange between coil, and the axle of little coiled type carbon element becomes the hollow form coil, along with the growth of little coil moves down substrate.
6. part or all is metallized into the manufacture method of the little coil of hollow ceramic, it is characterized in that: under the 700-1800 ℃ of high temperature, in containing the gas of metallic atom, with the little coil of hollow carbon element or hollow carbon cellulose fiber gas phase coated metal or carbonization treatment.State
7. the manufacture method of the little coil of hollow ceramic as claimed in claim 6, gas are the gas of nitrogen atom.
8. as the manufacture method of claim 6 or the little coil of 7 described hollow ceramic, containing metal, silicon, boron, carbon and/or containing in the gas of oxygen atom gas, high temperature is down with gas phase coated metal, silication, boronation, carbonization and or oxidation processes.
9. as any described manufacture method among the claim 6-8, part or all of little coil adjacent regions is fused into the hollow ceramic microfiber.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP208341/1997 | 1997-07-18 | ||
| JP20834197A JP3844564B2 (en) | 1997-07-18 | 1997-07-18 | Hollow microfiber and method for producing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1234840A true CN1234840A (en) | 1999-11-10 |
| CN1098941C CN1098941C (en) | 2003-01-15 |
Family
ID=16554677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN98801005A Expired - Fee Related CN1098941C (en) | 1997-07-18 | 1998-07-21 | Hollow microfiber and process for preparing same |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6368713B1 (en) |
| EP (1) | EP0943706B1 (en) |
| JP (1) | JP3844564B2 (en) |
| CN (1) | CN1098941C (en) |
| DE (1) | DE69830300T2 (en) |
| HK (1) | HK1020760A1 (en) |
| WO (1) | WO1999004073A1 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1113990C (en) * | 2000-06-07 | 2003-07-09 | 华侨大学 | High elastic screw carbon fibre and its preparing method |
| CN102383224A (en) * | 2011-11-14 | 2012-03-21 | 中国人民解放军国防科学技术大学 | Method of preparing carbon fibers through crosslinked reaction of boron trichloride and polyacrylonitrile precursors |
| CN103882536A (en) * | 2012-12-19 | 2014-06-25 | 财团法人工业技术研究院 | Hollow fiber for adsorption or filtration and method for producing the same |
| US9222200B2 (en) | 2012-12-19 | 2015-12-29 | Industrial Technology Research Institute | Spinning device |
| CN105979759A (en) * | 2016-07-18 | 2016-09-28 | 福建星宏新材料科技有限公司 | Wave-absorbing particle |
| CN115122714B (en) * | 2022-05-30 | 2023-09-22 | 安徽天富环保科技材料有限公司 | Preparation process of activated carbon fiber cloth for electrode preparation |
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|---|---|---|---|---|
| JP3844564B2 (en) * | 1997-07-18 | 2006-11-15 | 独立行政法人科学技術振興機構 | Hollow microfiber and method for producing the same |
| CN1328424C (en) * | 2004-04-23 | 2007-07-25 | 中国科学院理化技术研究所 | Micro carbon roll, process for preparing same and use thereof |
| JP5311105B2 (en) * | 2007-07-12 | 2013-10-09 | イマジニアリング株式会社 | Exhaust gas purification equipment |
| CZ301271B6 (en) * | 2008-05-06 | 2009-12-30 | Elmarco S.R.O. | Method for production of inorganic nanofibers and/or nanofibrous structures comprising TiN, inorganic nanofibers and/or nanofibrous structures comprising TiN and use of such nanofibrous structures |
| JP6342345B2 (en) * | 2015-02-09 | 2018-06-13 | 三菱重工業株式会社 | Method for producing metal nanocoil |
| CN106337217B (en) * | 2016-10-12 | 2018-12-28 | 中国人民解放军国防科学技术大学 | A kind of porous Si-B-N-O superfine fibre and preparation method thereof |
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| JPS59179875A (en) * | 1983-03-26 | 1984-10-12 | 工業技術院長 | Surface coated carbon fiber and production thereof |
| US6375917B1 (en) * | 1984-12-06 | 2002-04-23 | Hyperion Catalysis International, Inc. | Apparatus for the production of carbon fibrils by catalysis and methods thereof |
| US5165909A (en) * | 1984-12-06 | 1992-11-24 | Hyperion Catalysis Int'l., Inc. | Carbon fibrils and method for producing same |
| US5611964A (en) * | 1984-12-06 | 1997-03-18 | Hyperion Catalysis International | Fibril filled molding compositions |
| US4663230A (en) * | 1984-12-06 | 1987-05-05 | Hyperion Catalysis International, Inc. | Carbon fibrils, method for producing same and compositions containing same |
| US5171560A (en) * | 1984-12-06 | 1992-12-15 | Hyperion Catalysis International | Carbon fibrils, method for producing same, and encapsulated catalyst |
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| JP2662413B2 (en) * | 1988-04-12 | 1997-10-15 | 昭和電工株式会社 | Method for producing vapor grown carbon fiber |
| USH721H (en) * | 1988-07-05 | 1990-01-02 | The United States Of America As Represented By The Secretary Of The Air Force | Production of 10 micron diameter hollow ceramic fibers |
| US5011566A (en) * | 1989-03-15 | 1991-04-30 | The United States Of America As Represented By The Secretary Of The Air Force | Method of manufacturing microscopic tube material |
| ZA907803B (en) * | 1989-09-28 | 1991-07-31 | Hyperion Catalysis Int | Electrochemical cells and preparing carbon fibrils |
| JP2944246B2 (en) * | 1990-09-29 | 1999-08-30 | セントラル硝子株式会社 | Method for producing coiled carbon fiber |
| US5458784A (en) * | 1990-10-23 | 1995-10-17 | Catalytic Materials Limited | Removal of contaminants from aqueous and gaseous streams using graphic filaments |
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| EP0519641A1 (en) * | 1991-06-17 | 1992-12-23 | General Electric Company | Silicon carbide composite with coated fiber reinforcement and method of forming |
| JPH062269A (en) * | 1992-06-15 | 1994-01-11 | Osaka Gas Co Ltd | Method for coating carbon fiber and composite material |
| US5643670A (en) * | 1993-07-29 | 1997-07-01 | The Research Foundation Of State University Of New York At Buffalo | Particulate carbon complex |
| JPH07102423A (en) * | 1993-09-10 | 1995-04-18 | Hyperion Catalysis Internatl Inc | Graphite quality fibril material |
| JP2973352B2 (en) * | 1995-07-10 | 1999-11-08 | 科学技術振興事業団 | How to make graphite fiber |
| JPH09111135A (en) * | 1995-10-23 | 1997-04-28 | Mitsubishi Materials Corp | Conductive polymer composition |
| JPH09115334A (en) * | 1995-10-23 | 1997-05-02 | Mitsubishi Materiais Corp | Transparent conductive film and composition for film formation |
| US5853877A (en) * | 1996-05-31 | 1998-12-29 | Hyperion Catalysis International, Inc. | Method for disentangling hollow carbon microfibers, electrically conductive transparent carbon microfibers aggregation film amd coating for forming such film |
| JP3844564B2 (en) * | 1997-07-18 | 2006-11-15 | 独立行政法人科学技術振興機構 | Hollow microfiber and method for producing the same |
-
1997
- 1997-07-18 JP JP20834197A patent/JP3844564B2/en not_active Expired - Fee Related
-
1998
- 1998-07-21 EP EP19980932595 patent/EP0943706B1/en not_active Expired - Lifetime
- 1998-07-21 WO PCT/JP1998/003251 patent/WO1999004073A1/en active IP Right Grant
- 1998-07-21 DE DE1998630300 patent/DE69830300T2/en not_active Expired - Fee Related
- 1998-07-21 CN CN98801005A patent/CN1098941C/en not_active Expired - Fee Related
-
1999
- 1999-03-18 US US09/271,708 patent/US6368713B1/en not_active Expired - Fee Related
- 1999-11-16 HK HK99105278A patent/HK1020760A1/en not_active IP Right Cessation
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1113990C (en) * | 2000-06-07 | 2003-07-09 | 华侨大学 | High elastic screw carbon fibre and its preparing method |
| CN102383224A (en) * | 2011-11-14 | 2012-03-21 | 中国人民解放军国防科学技术大学 | Method of preparing carbon fibers through crosslinked reaction of boron trichloride and polyacrylonitrile precursors |
| CN102383224B (en) * | 2011-11-14 | 2013-11-06 | 中国人民解放军国防科学技术大学 | Method of preparing carbon fibers through crosslinked reaction of boron trichloride and polyacrylonitrile precursors |
| CN103882536A (en) * | 2012-12-19 | 2014-06-25 | 财团法人工业技术研究院 | Hollow fiber for adsorption or filtration and method for producing the same |
| US9222200B2 (en) | 2012-12-19 | 2015-12-29 | Industrial Technology Research Institute | Spinning device |
| CN105979759A (en) * | 2016-07-18 | 2016-09-28 | 福建星宏新材料科技有限公司 | Wave-absorbing particle |
| CN115122714B (en) * | 2022-05-30 | 2023-09-22 | 安徽天富环保科技材料有限公司 | Preparation process of activated carbon fiber cloth for electrode preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69830300T2 (en) | 2006-02-02 |
| EP0943706B1 (en) | 2005-05-25 |
| EP0943706A4 (en) | 1999-12-08 |
| EP0943706A1 (en) | 1999-09-22 |
| HK1020760A1 (en) | 2000-05-19 |
| WO1999004073A1 (en) | 1999-01-28 |
| CN1098941C (en) | 2003-01-15 |
| JP3844564B2 (en) | 2006-11-15 |
| JPH1143827A (en) | 1999-02-16 |
| US6368713B1 (en) | 2002-04-09 |
| DE69830300D1 (en) | 2005-06-30 |
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